Article Text
Abstract
The use of prisoners as research participants is controversial. Efforts to protect them in response to past exploitation and abuse have led to strict regulations and reluctance to involve them as participants. Hence, prisoners are routinely denied the opportunity to participate in research. In the absence of comprehensive information regarding prisoners’ current involvement in research, we examined UK prisoners’ involvement through review of research applications to the UK National Research Ethics Service. We found that prisoners have extremely limited access to research participation. This analysis was augmented by a survey of those involved in research and research governance (UK researchers and Research Ethics Committee members). Our results suggest that pragmatic concerns regarding the perceived burden of including prisoners are far more prominent in motivating their exclusion than ethical concerns or knowledge of regulations. While prisoners may remain a vulnerable research population due to constraints upon their liberty and autonomy and the coercive nature of the prison environment, routine exclusion from participation may be disadvantageous. Rigorous ethical oversight and the shift in the prevailing attitude towards the risks and benefits of participation suggest that it may be time for research to be more accessible to prisoners in line with the principle of equivalence in prison healthcare. We suggest the necessary first step in this process is a re-examination of current guidance in the UK and other countries with exclusions.
- Prisoners
- Research Ethics
- Research on Special Populations
Statistics from Altmetric.com
Read the full text or download the PDF:
Other content recommended for you
- Quantitative valuation placed by children and teenagers on participation in two hypothetical research scenarios
- Applying for ethical approval for research in the United Kingdom
- Results of a self-assessment tool to assess the operational characteristics of research ethics committees in low- and middle-income countries
- Researching about us without us: exploring research participation and the politics of disability rights in the context of the Mental Capacity Act 2005
- Standards for research ethics committees: purpose, problems and the possibilities of other approaches
- More guidelines on research ethics?
- Lay REC members: patient or public?
- Assent in paediatric research: theoretical and practical considerations
- ‘The ethics approval took 20 months on a trial which was meant to help terminally ill cancer patients. In the end we had to send the funding back’: a survey of views on human research ethics reviews
- Inclusion of adults with conditions that have the potential to affect capacity and or communication in research: triangulation from a mixed-methods study of current practice and values across multiple stakeholders